rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
1997-3-25
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pubmed:abstractText |
In a European, prospective, 1:2 randomized phase II multicentre study, 237 patients with advanced or metastatic prostate cancer were treated with either the 1M- (80 patients) or 3M-depot formulation (157 patients) of leuprorelin acetate for 9 months to compare efficacy and safety.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0302-2838
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
30 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7-14; discussion 19-21
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8977984-Aged,
pubmed-meshheading:8977984-Antineoplastic Agents, Hormonal,
pubmed-meshheading:8977984-Delayed-Action Preparations,
pubmed-meshheading:8977984-Gonadotropins,
pubmed-meshheading:8977984-Humans,
pubmed-meshheading:8977984-Leuprolide,
pubmed-meshheading:8977984-Male,
pubmed-meshheading:8977984-Prostate-Specific Antigen,
pubmed-meshheading:8977984-Prostatic Neoplasms,
pubmed-meshheading:8977984-Testosterone,
pubmed-meshheading:8977984-Time Factors
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pubmed:year |
1996
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pubmed:articleTitle |
Randomized open labelled comparative study of the efficacy, safety and tolerability of leuprorelin acetate 1M and 3M depot in patients with advanced prostatic cancer.
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pubmed:affiliation |
Urological Clinic, University of Tübingen, Germany.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Randomized Controlled Trial,
Multicenter Study,
Clinical Trial, Phase II
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